Baskin D S, Hosobuchi Y, Grevel J C
J Neurosurg. 1986 Jan;64(1):99-103. doi: 10.3171/jns.1986.64.1.0099.
The effects are reported of acute and long-term continuous administration of three opiate antagonists--naloxone, naltrexone, and diprenorphine--on neurological function, survival, and infarct size in a feline model of acute focal cerebral ischemia. All three drugs produced statistically significant improvement in motor function following acute administration without concomitant changes in level of consciousness; saline had no effect. Naloxone and naltrexone significantly prolonged survival (p less than 0.01); diprenorphine did not. Infarct size was not altered by any treatment administered. These findings confirm previous work suggesting that, with the appropriate methodology, treatment with opiate antagonists partially reverses neurological deficits. They also show that opiate antagonists prolong survival in certain conditions of acute and subacute focal cerebral ischemia without altering the area of infarcted tissue.
在猫急性局灶性脑缺血模型中,报告了三种阿片拮抗剂——纳洛酮、纳曲酮和二丙诺啡——急性和长期连续给药对神经功能、存活率和梗死灶大小的影响。急性给药后,所有三种药物均使运动功能有统计学意义的改善,而意识水平无伴随变化;生理盐水无作用。纳洛酮和纳曲酮显著延长了存活时间(p<0.01);二丙诺啡则没有。任何治疗均未改变梗死灶大小。这些发现证实了先前的研究工作,提示采用适当的方法,阿片拮抗剂治疗可部分逆转神经功能缺损。它们还表明,在急性和亚急性局灶性脑缺血的某些情况下,阿片拮抗剂可延长存活时间,而不改变梗死组织的面积。